Canonical Allele Identifier: PA2826617038
Gene: ELN HGNC NCBI

Linked Data

ClinVar Variation Id: 226631
ClinVar RCV Id: RCV000221492 RCV000417622 RCV000342594 RCV000376205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265845.1:p.Gly562Ser
CA4293247
NM_001278916.2:c.1684G>A